RecruitingADHDSleep DisturbanceBrain Fog
A Study to Evaluate the Effects of a Supplement on the Side Effects Associated With Stimulant Medications
Eligible age
18–55 yrs
Accepts
All genders
Locations
1 state
Healthy volunteers
Yes
See if you qualify for this study
Answer a few quick questions about your location and health. Takes about a minute.
About this study
This is a hybrid, two-arm, triple-blind, placebo-controlled, randomized clinical trial evaluating the efficacy of the Stasis supplement on reducing oxidative stress, cortisol levels, and side effects associated with stimulant medications used for ADHD over a three-month period in adults.
Sponsor: Outliers, Inc.
You may qualify if…
- ✓ Aged 18-55 years
- ✓ Currently prescribed stimulant medication for ADHD
- ✓ Experiencing: sleep difficulty, irritability, anxiety, brain fog
- ✓ Stable medication dose ≥3 months
- ✓ Healthy with no uncontrolled chronic conditions
- ✓ Stable on supplements ≥3 months if applicable
- ✓ US resident
- ✓ Willing to maintain current habits
You may not qualify if…
- ✕ Chronic conditions (e.g. cancer, mental illness)
- ✕ Use of psychiatric medications besides stimulants
- ✕ Pregnancy, breastfeeding, thyroid, liver, kidney conditions
- ✕ Recent smokers or heavy alcohol use
- ✕ Night shift workers
- ✕ Participation in other clinical trials
- ✕ Allergies to product ingredients
Where it's recruiting
Nevada
Las Vegas
Source: ClinicalTrials.gov · NCT07380412 · last updated 2026-02-02